Direct determination of arsenic in sea-water by reaction cell inductively coupled plasma mass spectrometry

被引:40
作者
Grotti, Marco [1 ]
Frache, Roberto [1 ]
机构
[1] Univ Genoa, Dept Chem & Ind Chem, I-16146 Genoa, Italy
关键词
D O I
10.1039/b711107j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new procedure for the direct determination of total arsenic in sea- water has been developed. In order to remove the polyatomic interferences arising from the direct analysis of 15- fold diluted sea- water samples, the dynamic reaction cell ( DRC) technique was applied. Different analytical strategies, such as reactive removal of the interfering species by ammonia, methane or hydrogen, as well as arsenic oxidation by oxygen or nitrogen protoxide, followed by detection of the AsO+ ion were explored. The use of DRC pressurized with ammonia, methane or hydrogen was not able to reduce the spectral interfering effects at m/ z = 75. On the other hand, satisfactory results were obtained by using oxygen at 0.8 cm(3) min(-1) or nitrogen protoxide at 0.5 cm(3) min(-1) and detecting the analyte at m/ z = 91. The relevant parameters, such as the reactive gas flow rate, the Mathieu stability parameters a and q of the DRC, and the rod offset voltages of both cell and mass analyzer quadrupole, were optimized for maximum ion transmission and selectivity. Following the optimization of the DRC conditions, a new analytical procedure for the direct determination of total arsenic concentration in sea- water was hence developed. The main analytical performance characteristics of the optimized method were evaluated, with special attention to the determination of the " procedural'' and "field'' blanks. A detection limit as low as 40 ng L-1 and instrumental precision of about 2% were achieved. The accuracy was verified by the analysis of certified reference materials ( CRM) of sea- water ( NASS- 4, CASS- 4) and estuarine water ( SLEW- 3). The analytical precision for replicated analyses of the CRMs ranged from 2.3% to 5.0% ( n = 5). Finally, the developed procedure was applied to a number of sea- water samples from the Ross Sea ( Southern Ocean, Antarctica). Arsenic concentration ranged from 0.88 to 1.03 mu g L-1 ( n = 12), which are typical values for the uncontaminated o. shore waters.
引用
收藏
页码:1481 / 1487
页数:7
相关论文
共 44 条
[1]   DETERMINATION OF ARSENIC SPECIES IN NATURAL-WATERS [J].
ANDREAE, MO .
ANALYTICAL CHEMISTRY, 1977, 49 (06) :820-823
[2]  
[Anonymous], TRACE ELEMENT SPECIA
[3]   Gas-phase ion-molecule reactions for resolution of atomic isobars: AMS and ICP-MS perspectives [J].
Bandura, Dmitry R. ;
Baranov, Vladimir I. ;
Litherland, A. E. ;
Tanner, Scott D. .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2006, 255 :312-327
[4]   Reaction chemistry and collisional processes in multipole devices for resolving isobaric interferences in ICP-MS [J].
Bandura, DR ;
Baranov, VI ;
Tanner, SD .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 2001, 370 (05) :454-470
[5]   Inductively coupled plasma mass spectrometer with axial field in a quadrupole reaction cell [J].
Bandura, DR ;
Baranov, VI ;
Tanner, SD .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2002, 13 (10) :1176-1185
[6]   A dynamic reaction cell for inductively coupled plasma mass spectrometry (ICP-DRC-MS) - Part 1. The rf-field energy contribution in thermodynamics of ion-molecule reactions [J].
Baranov, VI ;
Tanner, SD .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1999, 14 (08) :1133-1142
[7]   Speciation of major arsenic species in seawater by flow injection hydride generation atomic absorption spectrometry [J].
Cabon, JY ;
Cabon, N .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 2000, 368 (05) :484-489
[8]   Photolytic oxidation of As species for determination of total As (including the 'hidden' As fraction) in coastal seawater by hydride generation-atomic fluorescence spectrometry [J].
Castro, E. ;
Lavilla, I. ;
Bendicho, C. .
TALANTA, 2007, 71 (01) :51-55
[9]   THE DETERMINATION OF ARSENIC BY ELECTROTHERMAL ATOMIC-ABSORPTION SPECTROMETRY WITH A GRAPHITE-FURNACE .1. DIFFICULTIES IN THE DIRECT DETERMINATION [J].
CHAKRABORTI, D ;
DEJONGHE, W ;
ADAMS, F .
ANALYTICA CHIMICA ACTA, 1980, 119 (02) :331-340
[10]   Summer distribution of trace metals in the western sector of the Ross Sea, Antarctica [J].
Corami, F ;
Capodaglio, G ;
Turetta, C ;
Soggia, F ;
Magi, E ;
Grotti, M .
JOURNAL OF ENVIRONMENTAL MONITORING, 2005, 7 (12) :1256-1264